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Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients
Background: BRAF(V600E) mutation is associated with poor prognosis of colorectal cancer (CRC) patients, but the comparison of clinic-pathologic features between V600E and non-V600E mutation was not well-known in CRC patients. The aim of this study is to evaluate the clinical and pathological feature...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720726/ https://www.ncbi.nlm.nih.gov/pubmed/33330032 http://dx.doi.org/10.3389/fonc.2020.563407 |
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author | Guan, Wen-Long Qiu, Miao-Zhen He, Cai-Yun Yang, Li-Qiong Jin, Ying Wang, Zhi-Qiang Li, Yu-Hong Xu, Rui-Hua Wang, Feng-Hua |
author_facet | Guan, Wen-Long Qiu, Miao-Zhen He, Cai-Yun Yang, Li-Qiong Jin, Ying Wang, Zhi-Qiang Li, Yu-Hong Xu, Rui-Hua Wang, Feng-Hua |
author_sort | Guan, Wen-Long |
collection | PubMed |
description | Background: BRAF(V600E) mutation is associated with poor prognosis of colorectal cancer (CRC) patients, but the comparison of clinic-pathologic features between V600E and non-V600E mutation was not well-known in CRC patients. The aim of this study is to evaluate the clinical and pathological features, prognostic value of BRAF mutations in CRC. Methods: We conducted a retrospective study to characterize the clinical and pathological features and survival of patients with BRAF mutated CRC. Patients were classified according to BRAF status as BRAF(V600E) mutation and non-V600E mutations. Difference of characteristics and survival between the two groups was analyzed. Results: There was no significant difference in gender, family history, location of primary tumor, metastatic sites between patients with BRAF-V600E mutation and non-V600E mutations. Patients with V600E mutation were younger than those with non-V600E mutations (p = 0.002). Patients with BRAF(V600E) mutation showed a poorer outcome than those with non-V600E mutations (23.1 vs. 49.9 months, respectively, p = 0.0024). Lack of CDX2 expression was associated with worse prognosis (mOS: 9.4 m vs. not reached, respectively, p = 0.016). Status of V600E mutation did not affect the mPFS and ORR of first-line or second-line treatment. Conclusion: BRAF(V600E) mutation defines a distinct subgroup of CRC with worse prognosis. Lack of CDX2 expression is associated with poor OS. Status of V600E mutation did not affect the mPFS of first-line or second-line treatment. |
format | Online Article Text |
id | pubmed-7720726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77207262020-12-15 Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients Guan, Wen-Long Qiu, Miao-Zhen He, Cai-Yun Yang, Li-Qiong Jin, Ying Wang, Zhi-Qiang Li, Yu-Hong Xu, Rui-Hua Wang, Feng-Hua Front Oncol Oncology Background: BRAF(V600E) mutation is associated with poor prognosis of colorectal cancer (CRC) patients, but the comparison of clinic-pathologic features between V600E and non-V600E mutation was not well-known in CRC patients. The aim of this study is to evaluate the clinical and pathological features, prognostic value of BRAF mutations in CRC. Methods: We conducted a retrospective study to characterize the clinical and pathological features and survival of patients with BRAF mutated CRC. Patients were classified according to BRAF status as BRAF(V600E) mutation and non-V600E mutations. Difference of characteristics and survival between the two groups was analyzed. Results: There was no significant difference in gender, family history, location of primary tumor, metastatic sites between patients with BRAF-V600E mutation and non-V600E mutations. Patients with V600E mutation were younger than those with non-V600E mutations (p = 0.002). Patients with BRAF(V600E) mutation showed a poorer outcome than those with non-V600E mutations (23.1 vs. 49.9 months, respectively, p = 0.0024). Lack of CDX2 expression was associated with worse prognosis (mOS: 9.4 m vs. not reached, respectively, p = 0.016). Status of V600E mutation did not affect the mPFS and ORR of first-line or second-line treatment. Conclusion: BRAF(V600E) mutation defines a distinct subgroup of CRC with worse prognosis. Lack of CDX2 expression is associated with poor OS. Status of V600E mutation did not affect the mPFS of first-line or second-line treatment. Frontiers Media S.A. 2020-11-23 /pmc/articles/PMC7720726/ /pubmed/33330032 http://dx.doi.org/10.3389/fonc.2020.563407 Text en Copyright © 2020 Guan, Qiu, He, Yang, Jin, Wang, Li, Xu and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Guan, Wen-Long Qiu, Miao-Zhen He, Cai-Yun Yang, Li-Qiong Jin, Ying Wang, Zhi-Qiang Li, Yu-Hong Xu, Rui-Hua Wang, Feng-Hua Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title | Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title_full | Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title_fullStr | Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title_full_unstemmed | Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title_short | Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients |
title_sort | clinicopathologic features and prognosis of braf mutated colorectal cancer patients |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720726/ https://www.ncbi.nlm.nih.gov/pubmed/33330032 http://dx.doi.org/10.3389/fonc.2020.563407 |
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